Proposed Data Collection Submitted for Public Comment and Recommendations, 20161-20163 [2021-07838]

Download as PDF 20161 Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; 4. Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submissions of responses; and 5. Assess information collection costs. Proposed Project American Academy of Pediatrics (AAP) Neurodevelopmental Extension inform any needed changes in topics, procedures, or other aspects of the program. The purpose and use of the session evaluation data will be to assure that specific information is conveyed and understood by participants for each monthly session, ongoing improvement in identification and referral by participating pediatricians, and to inform subsequent neurodevelopmental ECHO projects. Data will be collected through secure email and will include monthly chart reviews, a monthly session evaluation survey, one overall program evaluation survey at the end of the project period, and one overall debriefing conference call at the end of the project. The target population is actively practicing pediatricians. Quantitative descriptive analyses are planned for the chart reviews. Qualitive data will be obtained from the session and program evaluation surveys, as well as the debriefing conference call. CDC requests approval for an estimated 496 annualized burden hours. for Community Health Outcomes (ECHO) Program on Children with Fetal Alcohol Spectrum Disorders (FASD)— New—National Center on Birth Defects and Developmental Disabilities (NCBDDD), Centers for Disease Control and Prevention (CDC). Background and Brief Description The purpose of this information collection is to monitor and evaluate the American Academy of Pediatrics (AAP) Neurodevelopmental Extension for Community Health Outcomes (ECHO) Program on Children with Fetal Alcohol Spectrum Disorders (FASD). The intent of the project is to improve practicing pediatrician capacity for identification and care of children with neurodevelopmental disorders, particularly prenatal exposure to alcohol, in the medical home. Evaluation information will be used to monitor any incorporation of presented materials or suggestions from ECHO sessions into participating pediatric practices. Feedback also will ESTIMATED ANNUALIZED BURDEN HOURS Type of respondents Pediatricians Pediatricians Pediatricians Pediatricians Number of responses Burden per response (minutes) Burden in hours ............... ............... ............... ............... Chart Review .......................................................... Session evaluation survey ..................................... Program evaluation survey .................................... Debriefing conference call ...................................... 15 15 15 15 160 8 1 1 12/60 5/60 5/60 60/60 480 10 1 15 Total ..................... ................................................................................. ........................ ........................ ........................ 496 Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2021–07840 Filed 4–15–21; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [60Day–21–21EE; Docket No. CDC–2021– 0033] Proposed Data Collection Submitted for Public Comment and Recommendations Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice with comment period. AGENCY: jbell on DSKJLSW7X2PROD with NOTICES Number of respondents Form name The Centers for Disease Control and Prevention (CDC), as part of its continuing effort to reduce public SUMMARY: VerDate Sep<11>2014 19:57 Apr 15, 2021 Jkt 253001 burden and maximize the utility of government information, invites the general public and other Federal agencies the opportunity to comment on a proposed and/or continuing information collection, as required by the Paperwork Reduction Act of 1995. This notice invites comment on a proposed information collection project titled Integrated Viral Hepatitis Surveillance and Prevention Funding for Health Departments. This new data collection is for viral hepatitis (VH) case reporting data collected from the National Notifiable Diseases Surveillance System (NNDSS) which provides the primary population-based data used to describe the epidemiology of VH in the United States and for annual reporting of surveillance, prevention, and epidemiology performance measures via an Annual Performance Report. CDC must receive written comments on or before June 15, 2021. DATES: PO 00000 Frm 00048 Fmt 4703 Sfmt 4703 You may submit comments, identified by Docket No. CDC–2021– 0033 by any of the following methods: • Federal eRulemaking Portal: Regulations.gov. Follow the instructions for submitting comments. • Mail: Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and Prevention, 1600 Clifton Road NE, MS–D74, Atlanta, Georgia 30329. Instructions: All submissions received must include the agency name and Docket Number. CDC will post, without change, all relevant comments to Regulations.gov. Please note: Submit all comments through the Federal eRulemaking portal (regulations.gov) or by U.S. mail to the address listed above. FOR FURTHER INFORMATION CONTACT: To request more information on the proposed project or to obtain a copy of the information collection plan and instruments, contact Jeffrey M. Zirger, Information Collection Review Office, Centers for Disease Control and ADDRESSES: E:\FR\FM\16APN1.SGM 16APN1 20162 Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices Prevention, 1600 Clifton Road NE, MS– D74, Atlanta, Georgia 30329; phone: 404–639–7118; Email: omb@cdc.gov. Under the Paperwork Reduction Act of 1995 (PRA) (44 U.S.C. 3501–3520), Federal agencies must obtain approval from the Office of Management and Budget (OMB) for each collection of information they conduct or sponsor. In addition, the PRA also requires Federal agencies to provide a 60-day notice in the Federal Register concerning each proposed collection of information, including each new proposed collection, each proposed extension of existing collection of information, and each reinstatement of previously approved information collection before submitting the collection to the OMB for approval. To comply with this requirement, we are publishing this notice of a proposed data collection as described below. The OMB is particularly interested in comments that will help: 1. Evaluate whether the proposed collection of information is necessary for the proper performance of the functions of the agency, including whether the information will have practical utility; 2. Evaluate the accuracy of the agency’s estimate of the burden of the proposed collection of information, including the validity of the methodology and assumptions used; 3. Enhance the quality, utility, and clarity of the information to be collected; 4. Minimize the burden of the collection of information on those who are to respond, including through the use of appropriate automated, electronic, mechanical, or other technological collection techniques or other forms of information technology, e.g., permitting electronic submissions of responses; and 5. Assess information collection costs. SUPPLEMENTARY INFORMATION: Proposed Project jbell on DSKJLSW7X2PROD with NOTICES Integrated Viral Hepatitis Surveillance and Prevention Funding for Health Departments—New—National Center for HIV/AIDS, Viral Hepatitis, STD, and TB Prevention (NCHHSTP), Centers for Disease Control and Prevention (CDC). VerDate Sep<11>2014 19:57 Apr 15, 2021 Jkt 253001 Background and Brief Description CDC is authorized under Sections 304 and 306 of the Public Health Service Act (42 U.S.C. 242b and 242k) to collect information on cases of viral hepatitis (VH). Data collected by the National Notifiable Diseases Surveillance System (NNDSS) are the primary data used to monitor the extent and characteristics of the VH burden in the United States. VH surveillance data are used to describe trends in VH incidence, prevalence, and characteristics of infected persons and are used widely at the federal, state, and local levels for planning and evaluating prevention programs and health-care services, and to allocate funding for prevention and care. In 2021, CDC is implementing activities under a new cooperative agreement Integrated Viral Hepatitis Surveillance and Prevention Funding for Health Departments (CDC–RFA– PS21–2103). Tools exist to prevent new cases of hepatitis A, B, and C, to treat people living with hepatitis B, and to cure people living with hepatitis C. Yet new cases of VH continue to rise, many people infected with VH remain undiagnosed, and far too many VHrelated deaths occur in the US each year. The purpose of the activities under a new cooperative agreement is to enable states to collect data to evaluate disease burden and trends and to analyze and disseminate that data to develop or refine recommendations, policies, and practices that will ultimately reduce the burden of VH in their jurisdictions. The goals of the activities are to reduce new VH infections, VH-related morbidity and mortality, and VH-related disparities and to establish comprehensive national VH surveillance, which are in accordance with the Division of Viral Hepatitis 2025 Strategic Plan. The activities of the new cooperative agreement are separated into two components (Component 1: Surveillance, and Component 2: Prevention), containing six strategies: 1.1, develop, implement, and maintain a plan to rapidly detect and respond to outbreaks for hepatitis A, B, and C; 1.2, collect, analyze, interpret, and disseminate data to characterize trends, and implement public health interventions for hepatitis A, acute PO 00000 Frm 00049 Fmt 4703 Sfmt 4703 hepatitis B and acute and chronic hepatitis C; 1.3 (contingent on available funding), collect, analyze, interpret, and disseminate data to characterize trends and implement public health interventions for chronic hepatitis B and perinatal hepatitis C; 2.1, support VH elimination planning and surveillance, and maximize access to testing, treatment, and prevention; 2.2 (contingent on available funding), increase access to HCV and HBV testing and referral to care in high-impact settings; and 2.3 (contingent on available funding), improve access to services preventing VH among persons who inject drugs. Contingent on funding, an optional component (Component 3: Special Projects) will support improved access to prevention, diagnosis, and treatment of viral, bacterial and fungal infections related to drug use in settings disproportionately affected by drug use. Performance measures will be monitored to assess recipient performance, including quality of data, effective program implementation, and accountability of funds. Data collection via the Annual Performance Report is used for program accountability and to inform performance improvement. Outbreak reporting will also be submitted throughout the year. These data, which complement case data as another key component of national viral hepatitis surveillance, are critical to determining both the level of viral hepatitis activity within a jurisdiction as well as the effectiveness of each jurisdiction’s approach to cluster and outbreak response. A standardized Case Report Form will be used for surveillance data collection submitted to the National Notifiable Diseases Surveillance System (NNDSS). De-identified data, including national VH surveillance data, will be submitted to CDC electronically per each jurisdiction’s usual mechanism. Recipients will submit other required quantitative and qualitative performance measure data annually via an Annual Performance Report and as needed for outbreak reporting. CDC requests approval for an estimated 6,688 annual burden hours. There are no other costs to respondents other than their time. E:\FR\FM\16APN1.SGM 16APN1 20163 Federal Register / Vol. 86, No. 72 / Friday, April 16, 2021 / Notices ESTIMATED ANNUALIZED BURDEN HOURS Type of respondent Health Health Health Health Health Health Departments Departments Departments Departments Departments Departments Average burden per response (in hours) Total annual burden (in hours) ...... ...... ...... ...... ...... ...... Viral Hepatitis Case Report Form ........................ APR: Component 1 .............................................. APR: Component 2 .............................................. APR: Component 3 .............................................. Initial Outbreak Report Form ............................... Outbreak Summary Report Form ........................ 51 59 59 14 59 59 381 1 1 1 2 2 20/60 1 1 1 20/60 20/60 6,477 59 59 14 39 39 Total ....................... .............................................................................. ........................ ........................ ........................ 6,688 Jeffrey M. Zirger, Lead, Information Collection Review Office, Office of Scientific Integrity, Office of Science, Centers for Disease Control and Prevention. [FR Doc. 2021–07838 Filed 4–15–21; 8:45 am] BILLING CODE 4163–18–P DEPARTMENT OF HEALTH AND HUMAN SERVICES Centers for Disease Control and Prevention [Docket No. CDC–2021–0042] Advisory Committee on Immunization Practices (ACIP) Centers for Disease Control and Prevention (CDC), Department of Health and Human Services (HHS). ACTION: Notice of meeting and request for comment. AGENCY: In accordance with the Federal Advisory Committee Act, the Centers for Disease Control and Prevention (CDC), announces the following meeting of the Advisory Committee on Immunization Practices (ACIP). This meeting is open to the public. The meeting will be webcast live via the World Wide Web. DATES: The meeting will be held on April 14, 2021, from 1:30 p.m. to 4:30 p.m., EDT (dates and times subject to change, see the ACIP website for updates: https://www.cdc.gov/vaccines/ acip/). Written comments must be received on or before April 16, 2021. ADDRESSES: For more information on ACIP please visit the ACIP website: https://www.cdc.gov/vaccines/acip/ index.html.You may submit comments, identified by Docket No. CDC–2021– 0042 by any of the following methods: • Federal eRulemaking Portal: https://www.regulations.gov. Follow the instructions for submitting comments. • Mail: Centers for Disease Control and Prevention, 1600 Clifton Road NE, SUMMARY: jbell on DSKJLSW7X2PROD with NOTICES Number of responses per respondent Number of respondents Form name VerDate Sep<11>2014 19:57 Apr 15, 2021 Jkt 253001 MS H24–8, Atlanta, GA 30329–4027, Attn: April 14, 2021 ACIP Meeting Instructions: All submissions received must include the Agency name and Docket Number. All relevant comments received in conformance with the https://www.regulations.gov suitability policy will be posted without change to https://www.regulations.gov, including any personal information provided. For access to the docket to read background documents or comments received, go to https://www.regulations.gov. FOR FURTHER INFORMATION CONTACT: Stephanie Thomas, ACIP Committee Management Specialist, Centers for Disease Control and Prevention, National Center for Immunization and Respiratory Diseases, 1600 Clifton Road NE, MS–H24–8, Atlanta, GA 30329– 4027; Telephone: 404–639–8367; Email: ACIP@cdc.gov. SUPPLEMENTARY INFORMATION: In accordance with 41 CFR 102–3.150(b), less than 15 calendar days’ notice is being given for this meeting due to the exceptional circumstances of the COVID–19 pandemic and rapidly evolving COVID–19 vaccine development and regulatory processes. The Secretary of Health and Human Services has determined that COVID–19 is a Public Health Emergency. A notice of this ACIP meeting has also been posted on CDC’s ACIP website at: https:// www.cdc.gov/vaccines/acip/. In addition, CDC has sent notice of this ACIP meeting by email to those who subscribe to receive email updates about ACIP. PURPOSE: The committee is charged with advising the Director, CDC, on the use of immunizing agents. In addition, under 42 U.S.C. 1396s, the committee is mandated to establish and periodically review and, as appropriate, revise the list of vaccines for administration to vaccine-eligible children through the Vaccines for Children (VFC) program, along with schedules regarding dosing interval, dosage, and contraindications to administration of vaccines. Further, PO 00000 Frm 00050 Fmt 4703 Sfmt 4703 under provisions of the Affordable Care Act, section 2713 of the Public Health Service Act, immunization recommendations of the ACIP that have been approved by the Director of the Centers for Disease Control and Prevention and appear on CDC immunization schedules must be covered by applicable health plans. MATTERS TO BE CONSIDERED: The agenda will include discussions on Janssen (Johnson & Johnson) COVID–19 Vaccine Safety. A recommendation vote(s) is scheduled. Agenda items are subject to change as priorities dictate. For more information on the meeting agenda visit https://www.cdc.gov/ vaccines/acip/meetings/meetingsinfo.html. Meeting Information: The meeting will be webcast live via the World Wide Web; for more information on ACIP please visit the ACIP website: https:// www.cdc.gov/vaccines/acip/. Public Participation Interested persons or organizations are invited to participate by submitting written views, recommendations, and data. Please note that comments received, including attachments and other supporting materials, are part of the public record and are subject to public disclosure. Comments will be posted on https://www.regulations.gov. Therefore, do not include any information in your comment or supporting materials that you consider confidential or inappropriate for public disclosure. If you include your name, contact information, or other information that identifies you in the body of your comments, that information will be on public display. CDC will review all submissions and may choose to redact, or withhold, submissions containing private or proprietary information such as Social Security numbers, medical information, inappropriate language, or duplicate/ near duplicate examples of a mass-mail campaign. CDC will carefully consider all comments submitted into the docket. E:\FR\FM\16APN1.SGM 16APN1

Agencies

[Federal Register Volume 86, Number 72 (Friday, April 16, 2021)]
[Notices]
[Pages 20161-20163]
From the Federal Register Online via the Government Publishing Office [www.gpo.gov]
[FR Doc No: 2021-07838]


-----------------------------------------------------------------------

DEPARTMENT OF HEALTH AND HUMAN SERVICES

Centers for Disease Control and Prevention

[60Day-21-21EE; Docket No. CDC-2021-0033]


Proposed Data Collection Submitted for Public Comment and 
Recommendations

AGENCY: Centers for Disease Control and Prevention (CDC), Department of 
Health and Human Services (HHS).

ACTION: Notice with comment period.

-----------------------------------------------------------------------

SUMMARY: The Centers for Disease Control and Prevention (CDC), as part 
of its continuing effort to reduce public burden and maximize the 
utility of government information, invites the general public and other 
Federal agencies the opportunity to comment on a proposed and/or 
continuing information collection, as required by the Paperwork 
Reduction Act of 1995. This notice invites comment on a proposed 
information collection project titled Integrated Viral Hepatitis 
Surveillance and Prevention Funding for Health Departments. This new 
data collection is for viral hepatitis (VH) case reporting data 
collected from the National Notifiable Diseases Surveillance System 
(NNDSS) which provides the primary population-based data used to 
describe the epidemiology of VH in the United States and for annual 
reporting of surveillance, prevention, and epidemiology performance 
measures via an Annual Performance Report.

DATES: CDC must receive written comments on or before June 15, 2021.

ADDRESSES: You may submit comments, identified by Docket No. CDC-2021-
0033 by any of the following methods:
     Federal eRulemaking Portal: Regulations.gov. Follow the 
instructions for submitting comments.
     Mail: Jeffrey M. Zirger, Information Collection Review 
Office, Centers for Disease Control and Prevention, 1600 Clifton Road 
NE, MS-D74, Atlanta, Georgia 30329.
    Instructions: All submissions received must include the agency name 
and Docket Number. CDC will post, without change, all relevant comments 
to Regulations.gov.
    Please note: Submit all comments through the Federal eRulemaking 
portal (regulations.gov) or by U.S. mail to the address listed above.

FOR FURTHER INFORMATION CONTACT: To request more information on the 
proposed project or to obtain a copy of the information collection plan 
and instruments, contact Jeffrey M. Zirger, Information Collection 
Review Office, Centers for Disease Control and

[[Page 20162]]

Prevention, 1600 Clifton Road NE, MS-D74, Atlanta, Georgia 30329; 
phone: 404-639-7118; Email: [email protected].

SUPPLEMENTARY INFORMATION: Under the Paperwork Reduction Act of 1995 
(PRA) (44 U.S.C. 3501-3520), Federal agencies must obtain approval from 
the Office of Management and Budget (OMB) for each collection of 
information they conduct or sponsor. In addition, the PRA also requires 
Federal agencies to provide a 60-day notice in the Federal Register 
concerning each proposed collection of information, including each new 
proposed collection, each proposed extension of existing collection of 
information, and each reinstatement of previously approved information 
collection before submitting the collection to the OMB for approval. To 
comply with this requirement, we are publishing this notice of a 
proposed data collection as described below.
    The OMB is particularly interested in comments that will help:
    1. Evaluate whether the proposed collection of information is 
necessary for the proper performance of the functions of the agency, 
including whether the information will have practical utility;
    2. Evaluate the accuracy of the agency's estimate of the burden of 
the proposed collection of information, including the validity of the 
methodology and assumptions used;
    3. Enhance the quality, utility, and clarity of the information to 
be collected;
    4. Minimize the burden of the collection of information on those 
who are to respond, including through the use of appropriate automated, 
electronic, mechanical, or other technological collection techniques or 
other forms of information technology, e.g., permitting electronic 
submissions of responses; and
    5. Assess information collection costs.

Proposed Project

    Integrated Viral Hepatitis Surveillance and Prevention Funding for 
Health Departments--New--National Center for HIV/AIDS, Viral Hepatitis, 
STD, and TB Prevention (NCHHSTP), Centers for Disease Control and 
Prevention (CDC).

Background and Brief Description

    CDC is authorized under Sections 304 and 306 of the Public Health 
Service Act (42 U.S.C. 242b and 242k) to collect information on cases 
of viral hepatitis (VH). Data collected by the National Notifiable 
Diseases Surveillance System (NNDSS) are the primary data used to 
monitor the extent and characteristics of the VH burden in the United 
States. VH surveillance data are used to describe trends in VH 
incidence, prevalence, and characteristics of infected persons and are 
used widely at the federal, state, and local levels for planning and 
evaluating prevention programs and health-care services, and to 
allocate funding for prevention and care.
    In 2021, CDC is implementing activities under a new cooperative 
agreement Integrated Viral Hepatitis Surveillance and Prevention 
Funding for Health Departments (CDC-RFA-PS21-2103). Tools exist to 
prevent new cases of hepatitis A, B, and C, to treat people living with 
hepatitis B, and to cure people living with hepatitis C. Yet new cases 
of VH continue to rise, many people infected with VH remain 
undiagnosed, and far too many VH-related deaths occur in the US each 
year. The purpose of the activities under a new cooperative agreement 
is to enable states to collect data to evaluate disease burden and 
trends and to analyze and disseminate that data to develop or refine 
recommendations, policies, and practices that will ultimately reduce 
the burden of VH in their jurisdictions. The goals of the activities 
are to reduce new VH infections, VH-related morbidity and mortality, 
and VH-related disparities and to establish comprehensive national VH 
surveillance, which are in accordance with the Division of Viral 
Hepatitis 2025 Strategic Plan.
    The activities of the new cooperative agreement are separated into 
two components (Component 1: Surveillance, and Component 2: 
Prevention), containing six strategies: 1.1, develop, implement, and 
maintain a plan to rapidly detect and respond to outbreaks for 
hepatitis A, B, and C; 1.2, collect, analyze, interpret, and 
disseminate data to characterize trends, and implement public health 
interventions for hepatitis A, acute hepatitis B and acute and chronic 
hepatitis C; 1.3 (contingent on available funding), collect, analyze, 
interpret, and disseminate data to characterize trends and implement 
public health interventions for chronic hepatitis B and perinatal 
hepatitis C; 2.1, support VH elimination planning and surveillance, and 
maximize access to testing, treatment, and prevention; 2.2 (contingent 
on available funding), increase access to HCV and HBV testing and 
referral to care in high-impact settings; and 2.3 (contingent on 
available funding), improve access to services preventing VH among 
persons who inject drugs. Contingent on funding, an optional component 
(Component 3: Special Projects) will support improved access to 
prevention, diagnosis, and treatment of viral, bacterial and fungal 
infections related to drug use in settings disproportionately affected 
by drug use.
    Performance measures will be monitored to assess recipient 
performance, including quality of data, effective program 
implementation, and accountability of funds. Data collection via the 
Annual Performance Report is used for program accountability and to 
inform performance improvement.
    Outbreak reporting will also be submitted throughout the year. 
These data, which complement case data as another key component of 
national viral hepatitis surveillance, are critical to determining both 
the level of viral hepatitis activity within a jurisdiction as well as 
the effectiveness of each jurisdiction's approach to cluster and 
outbreak response.
    A standardized Case Report Form will be used for surveillance data 
collection submitted to the National Notifiable Diseases Surveillance 
System (NNDSS). De-identified data, including national VH surveillance 
data, will be submitted to CDC electronically per each jurisdiction's 
usual mechanism. Recipients will submit other required quantitative and 
qualitative performance measure data annually via an Annual Performance 
Report and as needed for outbreak reporting. CDC requests approval for 
an estimated 6,688 annual burden hours. There are no other costs to 
respondents other than their time.

[[Page 20163]]



                                        Estimated Annualized Burden Hours
----------------------------------------------------------------------------------------------------------------
                                                                                      Average
                                                     Number of       Number of      burden per     Total annual
      Type of respondent            Form name       respondents    responses per   response  (in    burden  (in
                                                                    respondent        hours)          hours)
----------------------------------------------------------------------------------------------------------------
Health Departments............  Viral Hepatitis               51             381           20/60           6,477
                                 Case Report
                                 Form.
Health Departments............  APR: Component 1              59               1               1              59
Health Departments............  APR: Component 2              59               1               1              59
Health Departments............  APR: Component 3              14               1               1              14
Health Departments............  Initial Outbreak              59               2           20/60              39
                                 Report Form.
Health Departments............  Outbreak Summary              59               2           20/60              39
                                 Report Form.
                                                 ---------------------------------------------------------------
    Total.....................  ................  ..............  ..............  ..............           6,688
----------------------------------------------------------------------------------------------------------------


Jeffrey M. Zirger,
Lead, Information Collection Review Office, Office of Scientific 
Integrity, Office of Science, Centers for Disease Control and 
Prevention.
[FR Doc. 2021-07838 Filed 4-15-21; 8:45 am]
BILLING CODE 4163-18-P


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